N-(3-(dimethylamino)propyl)-2-(4-azidophenyl)oxazole-4-carboxamide | 1353130-65-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: N-(3-(dimethylamino)propyl)-2-(4-azidophenyl)oxazole-4-carboxamide
• CAS: 1353130-65-0
• 化学式: C₁₅H₁₈N₆O₂
• 分子量: 314.347
• InChiKey: MTXMNHGCQOUYEL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.96
• 重原子数：
  23.0
• 可旋转键数：
  7.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  107.13
• 氢给体数：
  1.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  N-(3-(dimethylamino)propyl)-2-(4-azidophenyl)oxazole-4-carboxamide 、 N-(3-(dimethylamino)propyl)-2-(4-ethynylphenyl)oxazole-4-carboxamide 在 copper(ll) sulfate pentahydrate 、 sodium ascorbate 作用下， 以 水 、 叔丁醇 为溶剂， 反应 0.42h， 以69%的产率得到1,4-bis-(4-(4-(3-(dimethylamino)propylaminocarbonyl)oxazol-2-yl)phenyl)-1,2,3-triazole
  参考文献：
  名称：

  A fragment based click chemistry approach towards hybrid G-quadruplex ligands: design, synthesis and biophysical evaluation

  摘要：

  A library of hybrid oxazole-triazole based compounds containing contiguously linked aromatic units were synthesised as G-quadruplex binding ligands. The design of these ligands was based upon combining features of our first generation of G-quadruplex bis-triazole ligands and the natural product telomestatin. The syntheses and biophysical studies of these ligands are described. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.10.066
• 作为产物：
  描述：

  4-azidobenzamide 在 草酰氯 、 碳酸氢钠 、 lithium hydroxide 作用下， 以 四氢呋喃 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 为溶剂， 生成 N-(3-(dimethylamino)propyl)-2-(4-azidophenyl)oxazole-4-carboxamide
  参考文献：
  名称：

  A fragment based click chemistry approach towards hybrid G-quadruplex ligands: design, synthesis and biophysical evaluation

  摘要：

  A library of hybrid oxazole-triazole based compounds containing contiguously linked aromatic units were synthesised as G-quadruplex binding ligands. The design of these ligands was based upon combining features of our first generation of G-quadruplex bis-triazole ligands and the natural product telomestatin. The syntheses and biophysical studies of these ligands are described. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.10.066